The S100P/RAGE signaling pathway regulates expression of microRNA-21 in colon cancer cells

被引:35
作者
Mercado-Pimentel, Melania E. [1 ,3 ]
Onyeagucha, Benjamin C. [1 ,2 ]
Li, Qing [1 ]
Pimentel, Angel C. [4 ]
Jandova, Jana [1 ,3 ]
Nelson, Mark A. [1 ,2 ,3 ]
机构
[1] Univ Arizona, Dept Pathol, Tucson, AZ 85724 USA
[2] Univ Arizona, Canc Biol Grad Program, Tucson, AZ 85724 USA
[3] Univ Arizona, Ctr Canc, Tucson, AZ 85724 USA
[4] Univ Arizona, Dept Mol & Cell Biol, Tucson, AZ 85724 USA
关键词
Colon cancer; Metastasis; Inflammation; microRNAs; miR-21; RAGE; RECK; AP-1; TCGA; METASTASIS; MIR-21; ACTIVATION; RECEPTOR; RECK; GROWTH;
D O I
10.1016/j.febslet.2015.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S100P signaling through the receptor for advanced glycation end-products (RAGE) contributes to colon cancer invasion and metastasis, but the mechanistic features of this process are obscure. Here, we investigate whether activation of S100P/RAGE signaling regulates oncogenic microRNA-21 (miR-21). We show that exogenous S100P up-regulates miR-21 levels in human colon cancer cells, whereas knockdown of S100P results in a decrease of miR-21. Furthermore, blockage of RAGE with anti-RAGE antibody suppresses S100P induction of miR-21. In addition, we found that S100P induction of miR-21 expression involves ERK and is suppressed by the MEK inhibitor U0126. Also, S100P treatment stimulates the enrichment of c-Fos, and AP-1 family members, at the miR-21 gene promoter. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2388 / 2393
页数:6
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